A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449665



Internal ID227896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151660998..151771893hg38UCSC Ensembl
chr3:151378786..151489681hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38110896
hg19110896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941188
Samples
Known GenesAADACL2, LOC201651, MIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449665
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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